lithium carbonate lithium carbonate

Generic: lithium carbonate

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate lithium carbonate
Generic Name lithium carbonate
Labeler alembic pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

lithium carbonate 150 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-013
Product ID 62332-013_b1af5294-98eb-4c2c-9178-a057386fb3f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079159
Listing Expiration 2026-12-31
Marketing Start 2016-12-27

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332013
Hyphenated Format 62332-013

Supplemental Identifiers

RxCUI
197889 197893 311355
UPC
0362332015306 0362332013302 0362332014309
UNII
2BMD2GNA4V

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lithium carbonate lithium carbonate (source: ndc)
Generic Name lithium carbonate (source: ndc)
Application Number ANDA079159 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (62332-013-30)
  • 100 CAPSULE in 1 BOTTLE (62332-013-31)
  • 500 CAPSULE in 1 BOTTLE (62332-013-71)
  • 1000 CAPSULE in 1 BOTTLE (62332-013-91)
source: ndc

Packages (4)

62332-013-30 30 CAPSULE in 1 BOTTLE (62332-013-30) 62332-013-31 100 CAPSULE in 1 BOTTLE (62332-013-31) 62332-013-71 500 CAPSULE in 1 BOTTLE (62332-013-71) 62332-013-91 1000 CAPSULE in 1 BOTTLE (62332-013-91)

Ingredients (1)

lithium carbonate (150 mg/1)

Linked Drug Pages (1)

LITHIUM CARBONATE LITHIUM CARBONATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b1af5294-98eb-4c2c-9178-a057386fb3f7", "openfda": {"upc": ["0362332015306", "0362332013302", "0362332014309"], "unii": ["2BMD2GNA4V"], "rxcui": ["197889", "197893", "311355"], "spl_set_id": ["4ca2b977-b94c-4232-9b7e-835db97c9544"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62332-013-30)", "package_ndc": "62332-013-30", "marketing_start_date": "20161227"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62332-013-31)", "package_ndc": "62332-013-31", "marketing_start_date": "20161227"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (62332-013-71)", "package_ndc": "62332-013-71", "marketing_start_date": "20161227"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62332-013-91)", "package_ndc": "62332-013-91", "marketing_start_date": "20161227"}], "brand_name": "LITHIUM CARBONATE LITHIUM CARBONATE", "product_id": "62332-013_b1af5294-98eb-4c2c-9178-a057386fb3f7", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "62332-013", "generic_name": "LITHIUM CARBONATE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LITHIUM CARBONATE", "brand_name_suffix": "LITHIUM CARBONATE", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "150 mg/1"}], "application_number": "ANDA079159", "marketing_category": "ANDA", "marketing_start_date": "20161227", "listing_expiration_date": "20261231"}